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学者姓名:肖龙强

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Ultrahigh-resolution, high interface contrast ionic homopolymers induced by acid-base mixed electrostatic interactions and nanopattern evolution SCIE
期刊论文 | 2025 , 16 (21) , 2506-2513 | POLYMER CHEMISTRY
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Abstract :

Ultrahigh-resolution polymer materials with good thermal stability and high interface contrast have a wide range of application prospects in photolithography and nanomanufacturing processes. Here, we report a series of comb-like homopolymers based on polystyrene sulfonate imidazolium salts (PSSM-(i)imi), achieving efficient self-assembly under solvent-free conditions and obtaining sub-3 nm hexagonally packed cylinders and sub-4 nm lamellar nanopatterns with high interface contrast. The sulfonic acid groups in the main chain of the homopolymers are connected to imidazole groups containing hydrophobic alkyl side chains through acid-base mixed electrostatic interactions. The electrostatic interactions enhance the incompatibility between the two functional groups, while the alkyl side chain can precisely control the domain spacing and nanostructure of the pattern, regardless of their molecular weight. Through the effect of temperature fields, the thermal stability and spatial orientation of the homopolymer nanostructures were further studied, promoting the practical application of nanopatterned materials.

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GB/T 7714 Weng, Sen , Lu, Zhen , Cai, Jingyu et al. Ultrahigh-resolution, high interface contrast ionic homopolymers induced by acid-base mixed electrostatic interactions and nanopattern evolution [J]. | POLYMER CHEMISTRY , 2025 , 16 (21) : 2506-2513 .
MLA Weng, Sen et al. "Ultrahigh-resolution, high interface contrast ionic homopolymers induced by acid-base mixed electrostatic interactions and nanopattern evolution" . | POLYMER CHEMISTRY 16 . 21 (2025) : 2506-2513 .
APA Weng, Sen , Lu, Zhen , Cai, Jingyu , Xiao, Longqiang , Wang, Kairui , Zhao, Rui et al. Ultrahigh-resolution, high interface contrast ionic homopolymers induced by acid-base mixed electrostatic interactions and nanopattern evolution . | POLYMER CHEMISTRY , 2025 , 16 (21) , 2506-2513 .
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Ultrahigh-resolution, high interface contrast ionic homopolymers induced by acid-base mixed electrostatic interactions and nanopattern evolution Scopus
期刊论文 | 2025 , 16 (21) , 2506-2513 | Polymer Chemistry
Ultrahigh-resolution, high interface contrast ionic homopolymers induced by acid-base mixed electrostatic interactions and nanopattern evolution EI
期刊论文 | 2025 , 16 (21) , 2506-2513 | Polymer Chemistry
Positively charged hydrophobic polymer foams via high internal phase emulsion polymerization followed by quaternization for effective oil-in-water emulsion separation SCIE
期刊论文 | 2025 , 13 (2) | JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING
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Abstract :

Oil/water separation of emulsion stands as one of the most arduous and challenging aspects in oily wastewater treatment which represents a perennial trouble for humanity. Herein, positively charged hydrophobic polymer foams (PCHPFs) were fabricated by water-in-oil (W/O) high internal phase emulsion (HIPE) polymerization followed by quaternization, employing 4-vinylbenzyl chloride (VBC) and 4-tert-butylstyrene (tBS) as the comonomers. The quaternization degree of PCHPFs which can be adjusted by varying the VBC/tBS ratio has an important influence on the emulsion separation performance based on the charge demulsification mechanism. The porous morphologies of PCHPFs were revealed by SEM. The successful fabrication of PCHPFs was confirmed by FTIR and XPS. As VBC/tBS ratio increased from 0.5:1-5:1, the emulsion separation efficiency of PCHPFs first increased to a maximum of 95.9 % at 2:1 and then decreased. Additionally, the PCHPFs demonstrated robust hydrophobicity (water contact angles > 143 degrees), exceptional oil-water selectivity, remarkable oil-water separation capability, coupled with a certain absorption capacity for various oils and organic solvents (5-14 g/g). Given these advantages, PCHPFs are anticipated to emerge as an ideal solution for emulsion separation. Most importantly, the methodology for generating PCHPFs via quaternization in this research offers an innovative avenue in the design of charge demulsification materials.

Keyword :

Charge demulsification Charge demulsification Emulsion separation Emulsion separation High internal phase emulsion High internal phase emulsion Positively charged hydrophobic polymer foams Positively charged hydrophobic polymer foams Quaternization Quaternization

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GB/T 7714 Xue, Jiahao , Zhao, Yulai , Cai, Jingyu et al. Positively charged hydrophobic polymer foams via high internal phase emulsion polymerization followed by quaternization for effective oil-in-water emulsion separation [J]. | JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING , 2025 , 13 (2) .
MLA Xue, Jiahao et al. "Positively charged hydrophobic polymer foams via high internal phase emulsion polymerization followed by quaternization for effective oil-in-water emulsion separation" . | JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING 13 . 2 (2025) .
APA Xue, Jiahao , Zhao, Yulai , Cai, Jingyu , Lu, Zhen , Xiao, Longqiang , Hou, Linxi . Positively charged hydrophobic polymer foams via high internal phase emulsion polymerization followed by quaternization for effective oil-in-water emulsion separation . | JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING , 2025 , 13 (2) .
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Positively charged hydrophobic polymer foams via high internal phase emulsion polymerization followed by quaternization for effective oil-in-water emulsion separation EI
期刊论文 | 2025 , 13 (2) | Journal of Environmental Chemical Engineering
Positively charged hydrophobic polymer foams via high internal phase emulsion polymerization followed by quaternization for effective oil-in-water emulsion separation Scopus
期刊论文 | 2025 , 13 (2) | Journal of Environmental Chemical Engineering
Hierarchical Co-C@PDA@BN/PAM composites: synergistic enhancement of microwave absorption and thermal conductivity through heterostructure design SCIE
期刊论文 | 2025 , 13 (24) , 12407-12419 | JOURNAL OF MATERIALS CHEMISTRY C
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The development of modern electronic devices necessitates the creation of materials that exhibit both excellent thermal conductivity and high electromagnetic wave absorption performance. This study focuses on the synthesis of a dual-functional composite material, Co-C@PDA@BN, by incorporating boron nitride (BN) onto a metal-organic framework (MOF)-derived Co-C core through the strong adhesion properties of polydopamine (PDA). The heterogeneous structural interface enhances interfacial polarization, thereby optimizing wave absorption. The thermal conductivity can be improved by adjusting the ratio of Co-C to BN. A composite with a Co-C to BN ratio of 1 : 5 shows a minimum reflection loss of -55.3 dB at 5 wt% and a thermal conductivity of 0.396 W m-1 K-1, while a ratio of 1 : 20 achieves a thermal conductivity value of 0.464 W m-1 K-1 with a minimum reflection loss of -44.9 dB, demonstrating the facile tunability of these two properties. This work provides a promising pathway via heterostructure design to balance thermal conductivity and wave absorption characteristics, which may offer guidance for advancing electronic device technology.

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GB/T 7714 Chen, Feng , Zhao, Hao , Xiao, Longqiang et al. Hierarchical Co-C@PDA@BN/PAM composites: synergistic enhancement of microwave absorption and thermal conductivity through heterostructure design [J]. | JOURNAL OF MATERIALS CHEMISTRY C , 2025 , 13 (24) : 12407-12419 .
MLA Chen, Feng et al. "Hierarchical Co-C@PDA@BN/PAM composites: synergistic enhancement of microwave absorption and thermal conductivity through heterostructure design" . | JOURNAL OF MATERIALS CHEMISTRY C 13 . 24 (2025) : 12407-12419 .
APA Chen, Feng , Zhao, Hao , Xiao, Longqiang , Yin, Xiangyu , Zhao, Yulai , Lu, Zhen et al. Hierarchical Co-C@PDA@BN/PAM composites: synergistic enhancement of microwave absorption and thermal conductivity through heterostructure design . | JOURNAL OF MATERIALS CHEMISTRY C , 2025 , 13 (24) , 12407-12419 .
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Hierarchical Co-C@PDA@BN/PAM composites: synergistic enhancement of microwave absorption and thermal conductivity through heterostructure design Scopus
期刊论文 | 2025 | Journal of Materials Chemistry C
One-step fabrication of porous anion exchange membranes for acid recovery breaking acid permeability-selectivity trade-off SCIE
期刊论文 | 2025 , 723 | JOURNAL OF MEMBRANE SCIENCE
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Abstract :

Diffusion dialysis (DD) presents a highly promising and cost-efficient approach for acid recovery, yet its performance is often hindered by the acid permeability of anion exchange membranes (AEMs). To address this challenge, a one-step approach has been developed to fabricate porous AEMs. Using brominated polyphenylene oxide (BPPO) as the porous base membrane, imidazole is employed for in-situ crosslinking and cationization. This approach not only retains the inherent porosity (>63.5 %) of the base membrane but also achieves an exceptionally thin selective layer (<0.3 mu m), thereby creating abundant free space volume. Through a concurrent enhancement of ion transport sites and crosslinking density, the membrane effectively breaks acid permeability-selectivity trade-off. The optimal IPPO-20h AEM demonstrates a remarkable increase in both the acid dialysis coefficient (U-H+ = 34.1 x 10(-3) m/h) and separation factor (S-H+/(Fe)2+ = 573.8) in the HCl/FeCl2 system, with enhancements of 4- and 31-fold, respectively, compared to the commercial DF120 AEM, at 25 degrees C. This high-performance AEM, synthesized via a straightforward and mild process, offers significant potential for large-scale acid recovery applications.

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GB/T 7714 Shao, Haiyang , Tan, Zhengke , Cheng, Yafei et al. One-step fabrication of porous anion exchange membranes for acid recovery breaking acid permeability-selectivity trade-off [J]. | JOURNAL OF MEMBRANE SCIENCE , 2025 , 723 .
MLA Shao, Haiyang et al. "One-step fabrication of porous anion exchange membranes for acid recovery breaking acid permeability-selectivity trade-off" . | JOURNAL OF MEMBRANE SCIENCE 723 (2025) .
APA Shao, Haiyang , Tan, Zhengke , Cheng, Yafei , Yue, Xiang'an , Yuan, Lei , Jian, Weixiong et al. One-step fabrication of porous anion exchange membranes for acid recovery breaking acid permeability-selectivity trade-off . | JOURNAL OF MEMBRANE SCIENCE , 2025 , 723 .
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One-step fabrication of porous anion exchange membranes for acid recovery breaking acid permeability–selectivity trade-off Scopus
期刊论文 | 2025 , 723 | Journal of Membrane Science
One-step fabrication of porous anion exchange membranes for acid recovery breaking acid permeability–selectivity trade-off EI
期刊论文 | 2025 , 723 | Journal of Membrane Science
Vanillin-derived co-curing agent for enhanced flame retardancy and mechanical properties in epoxy resin SCIE
期刊论文 | 2025 , 143 , 691-703 | JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
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Abstract :

Herein, we present the synthesis and characterization of a novel phosphorus-containing epoxy co-curing agent, ANVD, fabricated via a one-pot method utilizing vanillin, 1,5-diaminonaphthalene, and DOPO as raw materials. Structural analysis conducted through FTIR and NMR spectroscopy confirmed the composition of ANVD. Differential scanning calorimetry (DSC) results indicated ANVD has significant contribution to the curing crosslinking of DGEBA, resulting in a slightly decreased Tg value for EP/ANVD compared to EP/DOPO, albeit still notably higher. Thermogravimetric analysis (TGA) revealed a reduction in the T5% and Tmax values of EP/ANVD, yet ANVD's superior char-forming ability increased char residue mass at elevated temperatures. Combustion tests showcased the outstanding flame retardancy of EP/ANVD, with EP/ANVD-5 exhibiting a limiting oxygen index (LOI) value of 33.2 % and achieving a V-0 rating in the UL-94 test. Furthermore, EP/ANVD-5 displayed a notable decrease of 38.6 % and 32.1 % in pHRR and av-HRR, respectively, compared to pure EP, surpassing EP/DOPO with equivalent phosphorus content. Analysis of decomposition products in both condensed and gas phases revealed ANVD's role in forming dense and continuous expanded char layers during combustion, releasing phosphorus radicals and non-combustible gases, thus exhibiting dual-phase flame retardant effects. Additionally, EP/ANVD-3 exhibited enhanced mechanical properties, with tensile strength and modulus increasing from 68.5 MPa and 0.75 GPa to 76.5 MPa and 0.86 GPa, respectively, compared to pure EP. Overall, the introduction of the bio-based flame retardant ANVD presents promising opportunities for the utilization of bio-based materials in flame retardancy applications.

Keyword :

Co-curing agent Co-curing agent Epoxy resin Epoxy resin Flame retardancy Flame retardancy Phosphaphenanthrene Phosphaphenanthrene Vanillin Vanillin

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GB/T 7714 Luo, Yang , Huang, Lewen , Cai, Jingyu et al. Vanillin-derived co-curing agent for enhanced flame retardancy and mechanical properties in epoxy resin [J]. | JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY , 2025 , 143 : 691-703 .
MLA Luo, Yang et al. "Vanillin-derived co-curing agent for enhanced flame retardancy and mechanical properties in epoxy resin" . | JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY 143 (2025) : 691-703 .
APA Luo, Yang , Huang, Lewen , Cai, Jingyu , Jiang, Qing , Liao, Xiafeng , Zhang, Haowen et al. Vanillin-derived co-curing agent for enhanced flame retardancy and mechanical properties in epoxy resin . | JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY , 2025 , 143 , 691-703 .
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Vanillin-derived co-curing agent for enhanced flame retardancy and mechanical properties in epoxy resin EI
期刊论文 | 2025 , 143 , 691-703 | Journal of Industrial and Engineering Chemistry
Vanillin-derived co-curing agent for enhanced flame retardancy and mechanical properties in epoxy resin Scopus
期刊论文 | 2024 , 143 , 691-703 | Journal of Industrial and Engineering Chemistry
Efficient dispersion of high-content SiO2 particles across a broad pH range with anionic block copolymer in aqueous solution: An experiment and mechanism study EI
期刊论文 | 2025 , 429 | Journal of Molecular Liquids
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Abstract :

Dispersion of SiO2 particles in aqueous solutions using block copolymers remains challenging, particularly due to degradation in highly alkaline environments and difficulty in achieving high solid content. Herein, we report the synthesis of an anionic block copolymer, poly(glyceryl methacrylate-b-sodium p-styrenesulfonate) (PGGMA-b-PSSS), containing abundant hydroxyl groups, via reversible addition-fragmentation chain transfer (RAFT) polymerization of sodium p-styrenesulfonate and glycidyl methacrylate monomers. The hydroxyl groups in PGGMA-b-PSSS serve as anchoring points, producing a steric hindrance effect between SiO2 particles by interacting with silanol groups on the particle surface. Furthermore, electrostatic repulsion from the poly(sodium p-styrenesulfonate) block significantly enhances the dispersibility of PGGMA-b-PSSS in aqueous systems. A systematic investigation of the dispersibility of SiO2 particles was conducted under various compositions and concentrations of PGGMA-b-PSSS across a wide alkaline pH range. Our results show the effective dispersion of sub-micron and micron-sized SiO2 particles, achieving solid contents of up to 35 wt% over a wide pH range (3–13). © 2025 Elsevier B.V.

Keyword :

Alkalinity Alkalinity Anionic polymerization Anionic polymerization Block copolymers Block copolymers Dispersions Dispersions Living polymerization Living polymerization

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GB/T 7714 You, Jiejian , Jiang, Qing , Sun, Shihao et al. Efficient dispersion of high-content SiO2 particles across a broad pH range with anionic block copolymer in aqueous solution: An experiment and mechanism study [J]. | Journal of Molecular Liquids , 2025 , 429 .
MLA You, Jiejian et al. "Efficient dispersion of high-content SiO2 particles across a broad pH range with anionic block copolymer in aqueous solution: An experiment and mechanism study" . | Journal of Molecular Liquids 429 (2025) .
APA You, Jiejian , Jiang, Qing , Sun, Shihao , Lin, Xiaocheng , Sui, Jincheng , Liao, Xiafeng et al. Efficient dispersion of high-content SiO2 particles across a broad pH range with anionic block copolymer in aqueous solution: An experiment and mechanism study . | Journal of Molecular Liquids , 2025 , 429 .
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Efficient dispersion of high-content SiO2 particles across a broad pH range with anionic block copolymer in aqueous solution: An experiment and mechanism study Scopus
期刊论文 | 2025 , 429 | Journal of Molecular Liquids
Facile synthesis of carbon dioxide and UV light dual-responsive asymmetric tetrablock polymers SCIE
期刊论文 | 2024 , 205 | REACTIVE & FUNCTIONAL POLYMERS
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Abstract :

This work reports the synthesis of CO2/ultraviolet (UV) light dual-responsive CABC-type asymmetric tetrablock polymers (CABC-ATP) based on organocatalyzed reversible complexation-mediated radical polymerization (RCMP) with methyl methacrylate (MMA), 2-Propenoic acid, 2-methyl-4-methyl-2-oxo-2H-1-benzopyran-7-yl ester (CMMA), and 2-(dimethylamino)ethyl methacrylate (DMAEMA) as block monomers by three steps. The obtained CABC-ATP has controllable number average molecular weight (Mn) and narrow molecular weight distribution (Mw/Mn = 1.18-1.29). The hydrodynamic diameter and fluorescence intensity were measured using dynamic light scattering coupled with fluorescence assays. Notably, the vesicle volume increased from an initial measurement of 247.6 nm to 285.4 nm post-experiment. The initial fluorescence emission intensity recorded was 4971, which decreased to 1412 following the introduction of carbon dioxide for 20 min. Subsequently, the fluorescence intensity recovered to 5199 upon nitrogen exposure. The response behavior of CABC-ATP to UV light is due to the cross-linking of coumarin-based monomer, resulting in the change of fluorescence intensity at the macro level. Besides, the protonation of tertiary amine is promoted by the stimulation of CO2, generating of the change of vesicle volume at the micro level.

Keyword :

Asymmetric tetrablock polymers Asymmetric tetrablock polymers Dual-responsive polymer Dual-responsive polymer Photopolymer Photopolymer Photopolymerization Photopolymerization Self-assemble Self-assemble

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GB/T 7714 Deng, Chenhuai , Lin, Yuanhao , Ge, Xuehui et al. Facile synthesis of carbon dioxide and UV light dual-responsive asymmetric tetrablock polymers [J]. | REACTIVE & FUNCTIONAL POLYMERS , 2024 , 205 .
MLA Deng, Chenhuai et al. "Facile synthesis of carbon dioxide and UV light dual-responsive asymmetric tetrablock polymers" . | REACTIVE & FUNCTIONAL POLYMERS 205 (2024) .
APA Deng, Chenhuai , Lin, Yuanhao , Ge, Xuehui , Yang, Hongjie , Hou, Linxi , Xiao, Longqiang . Facile synthesis of carbon dioxide and UV light dual-responsive asymmetric tetrablock polymers . | REACTIVE & FUNCTIONAL POLYMERS , 2024 , 205 .
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Facile synthesis of carbon dioxide and UV light dual-responsive asymmetric tetrablock polymers Scopus
期刊论文 | 2024 , 205 | Reactive and Functional Polymers
Facile synthesis of carbon dioxide and UV light dual-responsive asymmetric tetrablock polymers EI
期刊论文 | 2024 , 205 | Reactive and Functional Polymers
Non-coalescence of nonidentical droplets in oil under a DC electric field SCIE
期刊论文 | 2024 , 70 (8) | AICHE JOURNAL
WoS CC Cited Count: 3
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Abstract :

Excessive electric field strength causes the droplets to contact but not coalesce, severely deteriorating the oil-water separation efficiency. The investigation of the non-coalescence of nonidentical droplets in oil under a DC electric field is conducted using high-speed photography. The effects of droplet volume ratio and interfacial tension ratio on the characteristics and critical parameters for droplet non-coalescence are systematically explored. The results show the critical electrocapillary number for the non-coalescence of nonidentical droplets and critical contact cone angle decreases as the volume sum increases or the interfacial tension ratio decreases, which is related to the competition between the resultant electric field force and the interfacial tension force. These results contribute to optimizing the operating parameters of the electric coalescer and improving the oil-water separation efficiency.

Keyword :

capillary pressure difference capillary pressure difference droplet droplet electric field electric field liquid bridge liquid bridge nonidentical non-coalescence nonidentical non-coalescence

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GB/T 7714 Huang, Xin , Chen, Mindan , Huang, Yunyun et al. Non-coalescence of nonidentical droplets in oil under a DC electric field [J]. | AICHE JOURNAL , 2024 , 70 (8) .
MLA Huang, Xin et al. "Non-coalescence of nonidentical droplets in oil under a DC electric field" . | AICHE JOURNAL 70 . 8 (2024) .
APA Huang, Xin , Chen, Mindan , Huang, Yunyun , Luo, Xiaoming , Teng, Lin , Xiao, Longqiang et al. Non-coalescence of nonidentical droplets in oil under a DC electric field . | AICHE JOURNAL , 2024 , 70 (8) .
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Non‐coalescence of nonidentical droplets in oil under a DC electric field
期刊论文 | 2024 , 70 (8) , n/a-n/a | AIChE Journal
Non-coalescence of nonidentical droplets in oil under a DC electric field EI
期刊论文 | 2024 , 70 (8) | AIChE Journal
Non-coalescence of nonidentical droplets in oil under a DC electric field Scopus
期刊论文 | 2024 , 70 (8) | AIChE Journal
Enhancement of ammonia corrosion resistance of coatings through improving dispersion and binding site of graphene oxide in silane coatings SCIE
期刊论文 | 2024 , 989 | JOURNAL OF ALLOYS AND COMPOUNDS
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Copper metal is essential to our production process, but it is highly corrosive in an ammonia environment and must be highly valued. Anti-corrosion coating is a simple and cost-effective method of preventing metal corrosion. In this study, a composite silane coating was prepared on copper using an impregnation method with mercaptopropyltriethoxysilane (TPTES) as the silane substrate and graphene oxide (GO) modified with isophorone diisocyanate (IPDI) or isocyanatopropyltriethoxysilane (IPTS) as filler to protect the copper from ammonia corrosion. The coating samples were hanging tested against ammonia corrosion by setting up two corrosive environments: ammonia gas and ammonia water. After 20 days of corrosion, the surfaces of the TPTES/ IPDI-GO and TPTES/IPTS-GO coatings remained unchanged under both ammonia environments and the corrosion rate was consistently low at 2-3 mu m/y. Additionally, the coating exhibited high protective qualities according to the electrochemical impedance spectroscopy (EIS) test in a 3.5% NaCl solution, which is attributed to the good dispersion that improves the densification and regularity of the coating. Meanwhile, IPTS-GO has a greater binding force with the coating matrix due to the increased number of reactive sites, resulting in further improved corrosion protection. This study provides an idea for research on ammonia-resistant coatings.

Keyword :

Ammonia corrosion Ammonia corrosion Binding site Binding site Graphene oxide Graphene oxide Silane coating Silane coating

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GB/T 7714 Xu, Jincai , Zhao, Rui , Sun, Shihao et al. Enhancement of ammonia corrosion resistance of coatings through improving dispersion and binding site of graphene oxide in silane coatings [J]. | JOURNAL OF ALLOYS AND COMPOUNDS , 2024 , 989 .
MLA Xu, Jincai et al. "Enhancement of ammonia corrosion resistance of coatings through improving dispersion and binding site of graphene oxide in silane coatings" . | JOURNAL OF ALLOYS AND COMPOUNDS 989 (2024) .
APA Xu, Jincai , Zhao, Rui , Sun, Shihao , Wu, Zhengxiong , Lu, Zhen , Xiao, Longqiang et al. Enhancement of ammonia corrosion resistance of coatings through improving dispersion and binding site of graphene oxide in silane coatings . | JOURNAL OF ALLOYS AND COMPOUNDS , 2024 , 989 .
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Enhancement of ammonia corrosion resistance of coatings through improving dispersion and binding site of graphene oxide in silane coatings Scopus
期刊论文 | 2024 , 989 | Journal of Alloys and Compounds
Enhancement of ammonia corrosion resistance of coatings through improving dispersion and binding site of graphene oxide in silane coatings EI
期刊论文 | 2024 , 989 | Journal of Alloys and Compounds
Preparation and photocatalytic CO2 reduction performance of Z-scheme g-C3N4/WO3•H2O EI CSCD PKU
期刊论文 | 2024 , 41 (4) , 858-864 and 871 | Fine Chemicals
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Composite material g-C3N4/WO3•H2O (CNW-1) was synthesized by hydrothermal reaction from graphite phase carbon nitride (g-C3N4) and sodium tungstate dihydrate. The composite material obtained was then characterized by XRD, XPS, SEM and TEM, and its visible light catalytic CO2 reduction performance at 298 K and 0.1 MPa was evaluated, the possible reaction mechanism was proposed. It was found that the yield of CO and CH4 could be regulated by adjusting the crystal water content in tungsten trioxide. CNW-1 had the highest yield of CH4 (0.33 μmol/g), while g-C3N4/WO3 (CNW) had the highest CO yield (0.67 μmol/g) after 10 h of reaction. This study provides an effective strategy for the selective reduction of CO2 to C1 compounds, and highlights the potential application of Z-scheme photocatalytic systems constructed from g-C3N4 semiconductor in the field of catalysis. © 2024 Fine Chemicals. All rights reserved.

Keyword :

Carbon dioxide Carbon dioxide Carbon nitride Carbon nitride Catalysis Catalysis Composite materials Composite materials Graphite Graphite Tungsten compounds Tungsten compounds

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GB/T 7714 Zhang, Jian , Weng, Sen , Shi, Junjie et al. Preparation and photocatalytic CO2 reduction performance of Z-scheme g-C3N4/WO3•H2O [J]. | Fine Chemicals , 2024 , 41 (4) : 858-864 and 871 .
MLA Zhang, Jian et al. "Preparation and photocatalytic CO2 reduction performance of Z-scheme g-C3N4/WO3•H2O" . | Fine Chemicals 41 . 4 (2024) : 858-864 and 871 .
APA Zhang, Jian , Weng, Sen , Shi, Junjie , Cai, Jingyu , Xiao, Longqiang . Preparation and photocatalytic CO2 reduction performance of Z-scheme g-C3N4/WO3•H2O . | Fine Chemicals , 2024 , 41 (4) , 858-864 and 871 .
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